Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 2.1.1.8 extracted from

  • Apelt, J.; Grassmann, S.; Ligneau, X.; Pertz, H.H.; Ganellin, C.R.; Arrang, J.M.; Schwartz, J.C.; Schunack, W.; Stark, H.
    Search for histamine H3 receptor antagonists with combined inhibitory potency at Ntau-methyltransferase: ether derivatives (2005), Pharmazie, 60, 97-106.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
(5'-amino-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-[4-(3-piperidin-1-yl-propoxy)-phenyl]-methanone 50% inhibition at 0.0020 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus
(5'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-[4-(3-piperidin-1-yl-propoxy)-phenyl]-methanone 50% inhibition at 0.0015 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus
(5-nitro-pyridin-2-yl)-[4-(3-piperidin-1-yl-propoxy)-benzyl]-amine 50% inhibition at 0.0042 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus
(5-nitro-pyridin-2-yl)-{2-[4-(3-piperidin-1-yl-propoxy)-phenyl]-ethyl}-amine 50% inhibition at 0.0028 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus
(5-nitro-pyridin-2-yl)-{3-[4-(3-piperidin-1-yl-propoxy)-phenyl]-propyl}-amine 50% inhibition at 0.0017 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus
(5-nitro-pyridin-2-yl)-{4-[4-(3-piperidin-1-yl-propoxy)-phenyl]-butyl}-amine 50% inhibition at 0.0017 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus
1-(3-(4-(3,4-dihydro-2H-pyrrol-5-yl)phenoxy)propyl)piperidine 50% inhibition at 0.0090 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus
2-(3-piperidin-1-ylpropoxy)-1,3-benzothiazole quinoline 50% inhibition at 0.021 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus
5-nitro-2-(3-piperidin-1-ylpropoxy)pyridine 50% inhibition at 0.034 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus
5-nitro-N-(4-(3-piperidin-1-ylpropoxy)phenyl)pyridin-2-amine 50% inhibition at 0.0038 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus
6-(3-piperidin-1-ylpropoxy)pyridin-3-amine 50% inhibition at 0.053 mM, simultaneously a potent H3 receptor ligand Rattus norvegicus
6-piperidin-1-yl-1-[4-(3-piperidin-1-yl-propoxy)-phenyl]-hexan-1-one 50% inhibition at 0.0089 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus
7-chloro-4-(3-piperidin-1-ylpropoxy)quinoline 50% inhibition at 0.0026 mM, simultaneously a potent H3 receptor ligand Rattus norvegicus
N2-[2-[4-(3-piperidin-1-yl-propoxy)-phenyl]-ethyl]-pyridine-2,5-diamine 50% inhibition at 0.00031 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus
N2-[3-[4-(3-piperidin-1-yl-propoxy)-phenyl]-propyl]-pyridine-2,5-diamine 50% inhibition at 0.0013 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus
N2-[4-[4-(3-piperidin-1-yl-propoxy)-phenyl]-butyl]-pyridine-2,5-diamine 50% inhibition at 0.00034 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus
[4-(3-piperidin-1-yl-propoxy)-phenyl]-(1-quinolin-4-yl-piperidin-4-yl)-methanone 50% inhibition at 0.00031 mM, simultaneously a highly potent H3 receptor ligand Rattus norvegicus

Organism

Organism UniProt Comment Textmining
Rattus norvegicus
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
kidney
-
Rattus norvegicus
-

Synonyms

Synonyms Comment Organism
Ntau-methyltransferase
-
Rattus norvegicus